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[3+2]Cycloaddition of Vinyl Cyclopropane and Hydroxylamines via Isocynate Intermediate toγ-Lactams 被引量:1
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作者 Xiaobing Huang Jingxun Yu Xinjun Luan 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2023年第16期1937-1942,共6页
Comprehensive Summary A general and efficient strategy for the synthesis ofγ-lactams has been reported.The hydroxylamines form Lossen rearrangement products of electron-deficient group migration with base and then un... Comprehensive Summary A general and efficient strategy for the synthesis ofγ-lactams has been reported.The hydroxylamines form Lossen rearrangement products of electron-deficient group migration with base and then undergo[3+2]cycloaddition reaction with vinyl cyclopropane,which could be performed with broad substrate scope,excellent functional group tolerance and high efficiency to produce the desired products.It also allowed further modification to other derivatives of theseγ-lactams. 展开更多
关键词 γ-Lactams HYDROXYLAMINES vinyi cyclopropane PD-CATALYZED [3+2]cycloaddition AMINATION Insertion Ring expansion
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